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Dermanson Müster Myoglobin Flax Reagent Group - Taiwan Registration 47175d1c6fbe447ac0aa29dae831f0d4

Access comprehensive regulatory information for Dermanson Müster Myoglobin Flax Reagent Group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 47175d1c6fbe447ac0aa29dae831f0d4 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS LIMITED.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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47175d1c6fbe447ac0aa29dae831f0d4
Registration Details
Taiwan FDA Registration: 47175d1c6fbe447ac0aa29dae831f0d4
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Device Details

Dermanson Müster Myoglobin Flax Reagent Group
TW: 德曼遜敏斯特肌紅蛋白弗列克斯試劑組
Risk Class 2
Cancelled

Registration Details

47175d1c6fbe447ac0aa29dae831f0d4

DHA00602335409

Company Information

United States

Product Details

This product is equipped with the Dimension Vista system to measure the concentration of myoglobin in human serum and plasma.

C Immunology and microbiology

C.5680 肌紅蛋白免疫試驗系統

import

Dates and Status

Mar 16, 2012

Mar 16, 2017

Dec 13, 2019

Cancellation Information

Logged out

許可證已逾有效期